地塞米松
医学
化学免疫疗法
免疫疗法
化疗
背景(考古学)
癌症
CD8型
临床试验
培美曲塞
T细胞
肿瘤科
内科学
药理学
免疫学
免疫系统
生物
古生物学
顺铂
作者
Alistair Cook,Alison M. McDonnell,Richard Lake,Anna K. Nowak
出处
期刊:OncoImmunology
[Informa]
日期:2015-09-16
卷期号:5 (3): e1066062-e1066062
被引量:74
标识
DOI:10.1080/2162402x.2015.1066062
摘要
The glucocorticoid (GC) steroid dexamethasone (Dex) is used as a supportive care co-medication for cancer patients undergoing standard care pemetrexed/platinum doublet chemotherapy. As trials for new cancer immunotherapy treatments increase in prevalence, it is important to track the immunological changes induced by co-medications commonly used in the clinic, but not specifically included in trial design or in pre-clinical models. Here, we document a number of Dex -induced immunological effects, including a large-scale lymphodepletive effect particularly affecting CD4+ T cells but also CD8+ T cells. The proportion of regulatory T cells within the CD4+ compartment did not change after Dex was administered, however a significant increase in proliferation and activation of regulatory T cells was observed. We also noted Dex -induced proportional changes in dendritic cell (DC) subtypes. We discuss these immunological effects in the context of chemoimmunotherapy strategies, and suggest a number of considerations to be taken into account when designing future studies where Dex and other GCs may be in use.
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